Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Color Diagnostics, |
RCV000584172 | SCV000690220 | likely benign | Hereditary cancer-predisposing syndrome | 2017-10-27 | criteria provided, single submitter | clinical testing | |
Invitae | RCV001446546 | SCV001649594 | likely benign | Hereditary nonpolyposis colorectal neoplasms | 2016-12-14 | criteria provided, single submitter | clinical testing | |
All of Us Research Program, |
RCV004002155 | SCV004837773 | likely benign | Lynch syndrome | 2023-10-02 | criteria provided, single submitter | clinical testing |